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Computer-assisted automated synthesis. III. Synthesis of substituted N-(carboxyalkyl) amino-acid tert-butyl ester derivatives
A versatile automated synthesis apparatus, equipped with a chemical artificial intelligence, was developed to prepare and isolate a wide variety of compounds. The apparatus was to the synthesis of substituted N-(carboxyalkyl)amino-acids. The apparatus [1,2] is composed of units for performing variou...
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
1991
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2547931/ https://www.ncbi.nlm.nih.gov/pubmed/18924904 http://dx.doi.org/10.1155/S1463924691000330 |
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author | Hayashi, Nobuyoshi Sugawara, Tohru Kato, Shinji |
author_facet | Hayashi, Nobuyoshi Sugawara, Tohru Kato, Shinji |
author_sort | Hayashi, Nobuyoshi |
collection | PubMed |
description | A versatile automated synthesis apparatus, equipped with a chemical artificial intelligence, was developed to prepare and isolate a wide variety of compounds. The apparatus was to the synthesis of substituted N-(carboxyalkyl)amino-acids. The apparatus [1,2] is composed of units for performing various tasks,for example reagent supply, reaction, purification and separation, each linked to a control system. All synthetic processes, including washing and drying of the apparatus after each synthetic run, were automatically performed from the mixing of the reactants to the isolation of the products as powders or crystals. The reaction of an amino-acid tertbutyl ester acetic acid salt with a 2-keto acid sodium salt produces an unstable intermediate, Schiff base, which is reduced with sodum cyanoborohydride to give a substituted N-(carboxyalkyl)aminoacid tert-butyl ester sodium salt. The equilibrium and the consecutive reactions were controlled by adding sodium cyanoborohydride using the artificial intelligence software, which contained novel kinetic equations [3] and substituent effects [4]. Substitued N-(carboxyalkyl)amino-acid tert-butyl esters, 90 derivatives, were automatically synthesized using the computerassisted automated synthesis apparatus. The syntheses were performed unattended 24 hours a day, except for supplying the raw materials, reagents and solvents. The apparatus is extremely valuable for synthesizing many derivatives of a particular compound. The configurations of the products were determined by circular dichroism measurements. |
format | Text |
id | pubmed-2547931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1991 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-25479312008-10-16 Computer-assisted automated synthesis. III. Synthesis of substituted N-(carboxyalkyl) amino-acid tert-butyl ester derivatives Hayashi, Nobuyoshi Sugawara, Tohru Kato, Shinji J Automat Chem Research Article A versatile automated synthesis apparatus, equipped with a chemical artificial intelligence, was developed to prepare and isolate a wide variety of compounds. The apparatus was to the synthesis of substituted N-(carboxyalkyl)amino-acids. The apparatus [1,2] is composed of units for performing various tasks,for example reagent supply, reaction, purification and separation, each linked to a control system. All synthetic processes, including washing and drying of the apparatus after each synthetic run, were automatically performed from the mixing of the reactants to the isolation of the products as powders or crystals. The reaction of an amino-acid tertbutyl ester acetic acid salt with a 2-keto acid sodium salt produces an unstable intermediate, Schiff base, which is reduced with sodum cyanoborohydride to give a substituted N-(carboxyalkyl)aminoacid tert-butyl ester sodium salt. The equilibrium and the consecutive reactions were controlled by adding sodium cyanoborohydride using the artificial intelligence software, which contained novel kinetic equations [3] and substituent effects [4]. Substitued N-(carboxyalkyl)amino-acid tert-butyl esters, 90 derivatives, were automatically synthesized using the computerassisted automated synthesis apparatus. The syntheses were performed unattended 24 hours a day, except for supplying the raw materials, reagents and solvents. The apparatus is extremely valuable for synthesizing many derivatives of a particular compound. The configurations of the products were determined by circular dichroism measurements. Hindawi Publishing Corporation 1991 /pmc/articles/PMC2547931/ /pubmed/18924904 http://dx.doi.org/10.1155/S1463924691000330 Text en Copyright © 1991 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Hayashi, Nobuyoshi Sugawara, Tohru Kato, Shinji Computer-assisted automated synthesis. III. Synthesis of substituted N-(carboxyalkyl) amino-acid tert-butyl ester derivatives |
title | Computer-assisted automated synthesis.
III. Synthesis of substituted N-(carboxyalkyl) amino-acid tert-butyl ester derivatives |
title_full | Computer-assisted automated synthesis.
III. Synthesis of substituted N-(carboxyalkyl) amino-acid tert-butyl ester derivatives |
title_fullStr | Computer-assisted automated synthesis.
III. Synthesis of substituted N-(carboxyalkyl) amino-acid tert-butyl ester derivatives |
title_full_unstemmed | Computer-assisted automated synthesis.
III. Synthesis of substituted N-(carboxyalkyl) amino-acid tert-butyl ester derivatives |
title_short | Computer-assisted automated synthesis.
III. Synthesis of substituted N-(carboxyalkyl) amino-acid tert-butyl ester derivatives |
title_sort | computer-assisted automated synthesis.
iii. synthesis of substituted n-(carboxyalkyl) amino-acid tert-butyl ester derivatives |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2547931/ https://www.ncbi.nlm.nih.gov/pubmed/18924904 http://dx.doi.org/10.1155/S1463924691000330 |
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